Variant #0000830776 (NC_000008.10:g.30922527T>A, NM_000553.4:c.452T>A (WRN))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.30922527T>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID WRN_000033
Frequency 2/13004
Freq. EA 2/8598
Freq. AA 0/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:29:29 +02:00 (CEST)
Date last edited 2013-05-04 14:37:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
WRN NM_000553.4 ?/? c.452T>A r.(?) p.(Phe151Tyr)